Canonical Allele Identifier: CA136832184
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs151341394

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354879del , CM000668.2:g.31354879del GRCh38
NC_000006.11:g.31322656del , CM000668.1:g.31322656del GRCh37
NC_000006.10:g.31430635del NCBI36
NG_023187.1:g.7335del

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3060-213del
ENST00000481849.6:n.2807del
ENST00000497377.6:n.2714del
ENST00000640094.2:c.896-213del ENSP00000491275.2:n.896-213del
ENST00000696558.1:c.1082-213del ENSP00000512716.1:n.1082-213del
ENST00000696559.1:c.1013-213del ENSP00000512717.1:n.1013-213del
ENST00000696560.1:c.1013-213del ENSP00000512718.1:n.1013-213del
ENST00000696561.1:c.1013-213del ENSP00000512719.1:n.1013-213del
ENST00000696562.1:c.1013-213del ENSP00000512720.1:n.1013-213del
ENST00000412585.7:c.1013-213del MANE Select ENSP00000399168.2:n.1013-213del
ENST00000640094.1:c.89-213del ENSP00000491275.1:n.89-213del
ENST00000412585.6:c.1013-213del ENSP00000399168.2:n.1013-213del
ENST00000497377.5:n.199del
NM_005514.6:c.1013-213del NP_005505.2:n.1013-213del
XM_011514556.1:c.1046-213del XP_011512858.1:n.1046-213del
XM_011514557.1:c.896-213del XP_011512859.1:n.896-213del
XR_926175.1:n.1452-213del
NM_005514.7:c.1013-213del NP_005505.2:n.1013-213del
NM_005514.8:c.1013-213del MANE Select NP_005505.2:n.1013-213del